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机译:涉及Sry相关基因Sox8的突变与人生殖异常的光谱有关
AP HP Dept Genet Med F-75012 Paris France;
CNRS Inst Pasteur Human Dev Genet UMR 3738 F-75724 Paris France;
CNRS Inst Pasteur Human Dev Genet UMR 3738 F-75724 Paris France;
UPMC Childrens Hosp Pittsburgh Div Pediat Endocrinol Pittsburgh PA 15224 USA;
UCL Great Ormond St Inst Child Hlth Genet &
Genom Med London WC1N 1EH England;
CNRS Inst Pasteur Human Dev Genet UMR 3738 F-75724 Paris France;
CNRS Inst Pasteur Human Dev Genet UMR 3738 F-75724 Paris France;
Univ Pittsburgh Sch Med Magee Womens Res Inst Dept Obstet Gynecol &
Reprod Sci Pittsburgh PA;
Univ Pittsburgh Sch Med Magee Womens Res Inst Dept Obstet Gynecol &
Reprod Sci Pittsburgh PA;
Univ Pittsburgh Sch Med Magee Womens Res Inst Dept Obstet Gynecol &
Reprod Sci Pittsburgh PA;
Rigshosp Univ Dept Growth &
Reprod DK-2100 Copenhagen Denmark;
Chinese Acad Sci Drug Discovery Pipeline Genome Regulat Lab Guangzhou 510530 Guangdong Peoples;
AP HP Dept Genet Med F-75012 Paris France;
AP HP Dept Genet Med F-75012 Paris France;
Inst Mutualiste Montsouris Dept Mere Enfant F-75014 Paris France;
Inst Mutualiste Montsouris Dept Anat Pathol F-75014 Paris France;
Hop Cochin Serv Endocrinol Paris France;
CHU Rennes Biol Reprod F-35033 Rennes France;
Univ Paris 06 UPMC INSERM Hop Armand Trousseau UMR S933 F-75012 Paris France;
Univ Paris 05 F-75019 Paris France;
Univ Milan Dept Clin Sci &
Community Hlth I-20122 Milan Italy;
Univ Milan Dept Clin Sci &
Community Hlth I-20122 Milan Italy;
Adm Nacl Lab Inst Salud ANLIS Dr Carlos G Malbran Ctr Nacl Genet Med C1428ADN Buenos Aires DF;
Adm Nacl Lab Inst Salud ANLIS Dr Carlos G Malbran Ctr Nacl Genet Med C1428ADN Buenos Aires DF;
Adm Nacl Lab Inst Salud ANLIS Dr Carlos G Malbran Ctr Nacl Genet Med C1428ADN Buenos Aires DF;
Natl Res Ctr Dept Clin Genet Cairo 12622 Egypt;
Inst Pasteur Morocco Human Genet Unit Casablanca 20250 Morocco;
Hop Femme Mere Enfant Genet Serv F-69677 Bron France;
Univ Dundee Sch Life Sci Ctr Dermatol &
Genet Med Dundee DD1 5EH Scotland;
Univ Dundee Sch Life Sci Ctr Dermatol &
Genet Med Dundee DD1 5EH Scotland;
Inst Pasteur Human Evolutionary Genet F-75724 Paris France;
Rigshosp Univ Dept Growth &
Reprod DK-2100 Copenhagen Denmark;
Chinese Acad Sci Drug Discovery Pipeline Genome Regulat Lab Guangzhou 510530 Guangdong Peoples;
UCL Great Ormond St Inst Child Hlth Genet &
Genom Med London WC1N 1EH England;
AP HP Dept Genet Med F-75012 Paris France;
CNRS Inst Pasteur Human Dev Genet UMR 3738 F-75724 Paris France;
CNRS Inst Pasteur Human Dev Genet UMR 3738 F-75724 Paris France;
机译:涉及Sry相关基因Sox8的突变与人生殖异常的光谱有关
机译:PTPN11基因突变的结果,导致Noonan综合征的心脏异常频谱。
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机译:涉及Sry相关基因Sox8的突变与人生殖异常的光谱有关
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